(R)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate

98%

Reagent Code: #230706
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CAS Number 167102-62-7

science Other reagents with same CAS 167102-62-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.34 g/mol
Formula C₁₃H₂₄N₂O₅
badge Registry Numbers
MDL Number MFCD09878778
thermostat Physical Properties
Boiling Point 349.7℃°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral oxazolidine core makes it valuable in asymmetric synthesis, where stereochemical control is critical. Commonly employed in the preparation of protease inhibitors and other medicinal agents requiring high enantiomeric purity. The carbamate and ester functionalities allow for selective derivatization, enabling its use in prodrug design and targeted drug delivery systems. Also utilized in combinatorial chemistry for generating compound libraries in drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,000.00
250mg
10-20 days ฿3,390.00
5g
10-20 days ฿32,020.00
1g
10-20 days ฿9,150.00
(R)-tert-Butyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral oxazolidine core makes it valuable in asymmetric synthesis, where stereochemical control is critical. Commonly employed in the preparation of protease inhibitors and other medicinal agents requiring high enantiomeric purity. The carbamate and ester functionalities allow for selective derivatization, enabling its use in prodrug design and targeted drug delivery systems.

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral oxazolidine core makes it valuable in asymmetric synthesis, where stereochemical control is critical. Commonly employed in the preparation of protease inhibitors and other medicinal agents requiring high enantiomeric purity. The carbamate and ester functionalities allow for selective derivatization, enabling its use in prodrug design and targeted drug delivery systems. Also utilized in combinatorial chemistry for generating compound libraries in drug discovery.

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